Environmental Monitoring Technician I
The Environmental Monitoring Technician I at Confidential Client is responsible for performing routine environmental monitoring activities within aseptic manufacturing environments to ensure product quality and compliance with cGMP and GLP standards. This role involves data collection, documentation, and collaboration with manufacturing teams to maintain a safe and compliant production environment. The position requires adherence to safety and quality protocols, effective communication, and flexibility to support manufacturing schedules.
About Careertakes
👉 Important disclosure: Careertakes is a third-party recruiting platform supporting this hiring process. If selected, you will be employed directly by our client, Scientific & QA.
Applicants for this role may also receive access to additional matched opportunities through the Careertakes platform.
What You’ll Do
Perform environmental monitoring tasks in an Aseptic Manufacturing Environment to help ensure the safety, quality, and compliance of manufactured products. You will work with QC and production teams to support routine monitoring, data entry, reporting, and aseptic practices.
- Gain understanding of cGMPs, GLPs, EHS and site/department policies and environmental monitoring concepts
- Perform routine weekly/monthly sampling (viable, non‑viable, water, ISO and batch process sampling)
- Enter, verify and review environmental monitoring data in databases/computerized systems accurately and promptly
- Author and review monthly/annual environmental monitoring reports
- Ensure monitoring supplies are available in the Aseptic Processing Area (APA) and QC Laboratory
- Support production/manufacturing team members as business partners in the APA
- Become qualified on aseptic gowning and participate in media-fill operations
- Perform and document aseptic observations and operator coaching per site aseptic practices
- Consistently follow proper documentation practices and site procedures
Qualifications
- Entry-level position: High School diploma/GED plus ~1 year experience or training, or equivalent combination of education and experience
- Willingness to learn and develop a career in pharmaceutical/biotech manufacturing and quality control
- Ability to read, understand, and execute instructions in site procedures
- Strong documentation, written and verbal communication skills
- Strong organizational skills and ability to multi-task across projects and activities
- Ability to obtain and maintain multiple technique proficiencies as required by site business needs
- Completion of required training, written exams and certifications
- Flexible to work temporarily on other shifts as business needs dictate
Preferred
- Associate or Bachelor’s degree in Life Sciences and prior experience
- Experience working in a GMP environment or Quality Control role in the pharmaceutical industry
Compensation & Benefits
- Hourly pay range: $19.18 to $31.97 per hour (as listed by the client for Rochester Hills, MI)
- Eligibility for overtime, weekend, holiday and other pay premiums depending on schedule and client policies
- Benefits may include retirement plan options, paid time off, paid caregiver/parental leave, and health benefits (medical, prescription, dental, vision) — actual packages are determined by the hiring client and aligned to the location of hire
- Relocation assistance may be available based on business needs and eligibility
Work Schedule & Location
- Location: On premise — Rochester Hills, MI (first shift; schedule flexibility required, including potential weekends as manufacturing needs dictate)
- This role requires U.S. work authorization at the time of hire. Visa sponsorship is not available for this role.
- Minimal travel for training/seminars may be required
Physical & Other Requirements
- Must be able to lift a minimum of 30 lbs
- Role involves lifting, bending, standing for periods of time, use of ladders and working within controlled environments
- Must not have a penicillin allergy (site-specific requirement)
- Able to maintain a neat and tidy workspace and adhere to site safety rules
Key Skills & Keywords
- Environmental monitoring
- Aseptic manufacturing support
- cGMP / GLP compliance
- QC laboratory data entry & reporting
- Viable and non‑viable particle monitoring
Equal Opportunity & Hiring Transparency
Careertakes and our client are Equal Opportunity Employers committed to building a diverse and inclusive workforce. We prohibit discrimination or harassment of any kind. To support a fair and efficient hiring process, AI tools may be used to assist with application review or resume screening. These tools do not replace human decision-making. Final hiring decisions are made by people.
If you have questions about how your data is used, please contact us directly.
Negotiate a higher salary! Check the salary ranges for this job type in your area.
View My Salary Range